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CD324 (E-Cadherin)
Overview
The CD324 (E-Caherin) antibody can be used for the flow cytometric identification and enumeration of CD324 (E-Cadherin)+ cells, e.g. human ES and iPS cells, carcinoma cells, human cells of epithelial origin.
Details
Background information
CD324, also known as E-Cadherin or cadherin-1, is a calcium dependent cell adhesion protein found in adherence junctions of epithelial cells, e.g., in colon, uterus, liver, keratinocytes etc. E-Cadherin also serves as a ligand for integrin alpha-E/beta-71. The epitope is expressed by a variety of carcinoma-derived cell lines such as MCF-7, HT-29, T-47D, NTERA-2, and 2102Ep. Loss of E-Cadherin is thought to enable metastasis by disrupting intercellular contacts—an early step in metastatic dissemination2. Furthermore, E-Cadherin is a marker of undifferentiated embryonic stem (ES) cells and induced pluripotent stem (iPS) cells3,4. For these cells, E-Cadherin plays a major role in conveying cell survival signals5.
Clone Isotype
67A4mouse IgG1
Further information
Stem Cell Research Brochure
[PDF; 3,8 MB]
Stem Cell Product List Sept 2011
[PDF; 709,8 KB]
Cancer Research Brochure
[PDF; 4,3 MB]
 
Human induced pluripotent stem (iPS) cells were stained with CD324 (E-Cadherin) antibodies conjugated to PE (A) or APC (B) and analyzed by flow cytometry using the MACSQuant® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. Right line represents CD324 (E-Cadherin) staining, left line represents isotype control.
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Details
Products
CD324-PE, human
- for 100 tests (1)
Download datasheet
130-095-413
Qty.:
 

CD324-APC, human
- for 100 tests (1)
Download datasheet
130-095-412
Qty.:
 

(1) One test corresponds to fluorescent labeling of up to 106 cells in a total volume of 100 μL.
Related products
ES and iPS Cell Separation
ES and iPS Cell Analysis
ES and iPS Cell Culture
Tumor Cell Separation
Tumor Cell Analysis
References
1. Higgins, J. M. et al. (1998). J. Cell Biol. 140: 197–210.
2. Onder, T. T. et al. (2008 Cancer Res. 68: 3645–3654.
3. Eastham, A. M. et al. (2007) Cancer Res. 67: 11254–11262.
4. Li, Z. et al. (2010) J. Phys. Chem. B. 114: 2894–2900.
5. Xu, Y. et al. (2010) Proc. Natl. Acad. Sci. U.S.A. 107: 5129–8134.
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